{"title":"运动通过调节IGF-1-Humanin通路改善d -半乳糖处理大鼠心功能障碍","authors":"Hesam Askarimoghadam, Farzaneh Rostamzadeh, Maryamossadat Mirtajaddini Goki, Elham Jafari, Mahboobeh Yeganeh-Hajahmadi","doi":"10.1155/jare/9949234","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction:</b> Humanin, a mitochondrial-derived peptide, decreases in the elderly. This study evaluated the effects of concurrent moderate-intensity endurance training (MIET) or high-intensity interval training (HIIT) with D-galactose injection on cardiac function, and the serum and heart levels of humanin and IGF-1 in Wistar male rats. <b>Methods:</b> Left ventricular systolic pressure (LVSP), left ventricular end diastolic pressure (LVEDP), ±maxdp/dt, contractility index (CI) and, Tau were monitored by PowerLab system in CTL, CTL + MIET, CTL + HIIT, D-gal, D-gal + MIET, and D-gal + HIIT groups. The histopathological score, fibrosis, and humanin and IGF-1 levels were measured with hematoxylin & eosin, Masson's trichrome, and enzyme-linked immunosorbent assay, respectively. <b>Results:</b> Histopathological score and heart fibrosis were reduced by HIIT and MIET in the D-gal group. LVSP, ±maxdp/dt, and CI were lower, while LVEDP and Tau were higher in the D-gal group than in the CTL group. MIET and HIIT alleviated the changes in LVSP, ±maxdp/dt, CI, LVEDP, and Tau. HIIT and MIET increased humanin levels in heart and serum of the D-gal group by modifying IGF-1 levels. <b>Conclusion:</b> The study suggests HIIT and MIET may improve cardiac function by regulating the IGF-1-humanin signaling pathway.</p>","PeriodicalId":14933,"journal":{"name":"Journal of Aging Research","volume":"2025 ","pages":"9949234"},"PeriodicalIF":2.1000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12496137/pdf/","citationCount":"0","resultStr":"{\"title\":\"Exercise Improves Cardiac Dysfunction in D-Galactose-Treated Rats by Regulation of IGF-1-Humanin Pathway.\",\"authors\":\"Hesam Askarimoghadam, Farzaneh Rostamzadeh, Maryamossadat Mirtajaddini Goki, Elham Jafari, Mahboobeh Yeganeh-Hajahmadi\",\"doi\":\"10.1155/jare/9949234\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction:</b> Humanin, a mitochondrial-derived peptide, decreases in the elderly. This study evaluated the effects of concurrent moderate-intensity endurance training (MIET) or high-intensity interval training (HIIT) with D-galactose injection on cardiac function, and the serum and heart levels of humanin and IGF-1 in Wistar male rats. <b>Methods:</b> Left ventricular systolic pressure (LVSP), left ventricular end diastolic pressure (LVEDP), ±maxdp/dt, contractility index (CI) and, Tau were monitored by PowerLab system in CTL, CTL + MIET, CTL + HIIT, D-gal, D-gal + MIET, and D-gal + HIIT groups. The histopathological score, fibrosis, and humanin and IGF-1 levels were measured with hematoxylin & eosin, Masson's trichrome, and enzyme-linked immunosorbent assay, respectively. <b>Results:</b> Histopathological score and heart fibrosis were reduced by HIIT and MIET in the D-gal group. LVSP, ±maxdp/dt, and CI were lower, while LVEDP and Tau were higher in the D-gal group than in the CTL group. MIET and HIIT alleviated the changes in LVSP, ±maxdp/dt, CI, LVEDP, and Tau. HIIT and MIET increased humanin levels in heart and serum of the D-gal group by modifying IGF-1 levels. <b>Conclusion:</b> The study suggests HIIT and MIET may improve cardiac function by regulating the IGF-1-humanin signaling pathway.</p>\",\"PeriodicalId\":14933,\"journal\":{\"name\":\"Journal of Aging Research\",\"volume\":\"2025 \",\"pages\":\"9949234\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12496137/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Aging Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/jare/9949234\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"GERIATRICS & GERONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Aging Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/jare/9949234","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
Exercise Improves Cardiac Dysfunction in D-Galactose-Treated Rats by Regulation of IGF-1-Humanin Pathway.
Introduction: Humanin, a mitochondrial-derived peptide, decreases in the elderly. This study evaluated the effects of concurrent moderate-intensity endurance training (MIET) or high-intensity interval training (HIIT) with D-galactose injection on cardiac function, and the serum and heart levels of humanin and IGF-1 in Wistar male rats. Methods: Left ventricular systolic pressure (LVSP), left ventricular end diastolic pressure (LVEDP), ±maxdp/dt, contractility index (CI) and, Tau were monitored by PowerLab system in CTL, CTL + MIET, CTL + HIIT, D-gal, D-gal + MIET, and D-gal + HIIT groups. The histopathological score, fibrosis, and humanin and IGF-1 levels were measured with hematoxylin & eosin, Masson's trichrome, and enzyme-linked immunosorbent assay, respectively. Results: Histopathological score and heart fibrosis were reduced by HIIT and MIET in the D-gal group. LVSP, ±maxdp/dt, and CI were lower, while LVEDP and Tau were higher in the D-gal group than in the CTL group. MIET and HIIT alleviated the changes in LVSP, ±maxdp/dt, CI, LVEDP, and Tau. HIIT and MIET increased humanin levels in heart and serum of the D-gal group by modifying IGF-1 levels. Conclusion: The study suggests HIIT and MIET may improve cardiac function by regulating the IGF-1-humanin signaling pathway.